JPS6230849A - Directly quenched and tempered steel having superior sscc resistance characteristic - Google Patents

Directly quenched and tempered steel having superior sscc resistance characteristic

Info

Publication number
JPS6230849A
JPS6230849A JP16861985A JP16861985A JPS6230849A JP S6230849 A JPS6230849 A JP S6230849A JP 16861985 A JP16861985 A JP 16861985A JP 16861985 A JP16861985 A JP 16861985A JP S6230849 A JPS6230849 A JP S6230849A
Authority
JP
Japan
Prior art keywords
steel
less
prior austenite
grain size
resistance
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP16861985A
Other languages
Japanese (ja)
Other versions
JPH049847B2 (en
Inventor
Chiaki Ouchi
大内 千秋
Masakazu Niikura
新倉 正和
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JFE Engineering Corp
Original Assignee
NKK Corp
Nippon Kokan Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NKK Corp, Nippon Kokan Ltd filed Critical NKK Corp
Priority to JP16861985A priority Critical patent/JPS6230849A/en
Publication of JPS6230849A publication Critical patent/JPS6230849A/en
Publication of JPH049847B2 publication Critical patent/JPH049847B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a steel having superior SSCC resistance characteristic by direct quenching and tempering by controlling the structure of a low-alloy steel by a direct quenching process. CONSTITUTION:The composition of a steel is composed of, by weight, 0.15-0.35% C, 0.01-0.5% Si, 0.4-2% Mn, 0.001-0.1% acid-sol. Al and the balance Fe with inevitable impurities. The steel is hot worked at the Ac3 transformation point or above, directly quenched and tempered at the Ac1 transformation point or below to form a tempered martensite structure contg. old austenite grains drawn in >=2 ratio R represented by a formula R=dL/dZ (where dL is the grain size of old austenite in the rolling direction and dZ is the grain size of old austenite in the thickness direction).

Description

【発明の詳細な説明】 (腫東上の利用分野) 本発明は直接焼入れ焼戻しによる耐硫化物応力腐食割れ
特性(以下耐5scc特性と称す)の優れた鋼に関する
ものである。
DETAILED DESCRIPTION OF THE INVENTION (Field of Application of Mado) The present invention relates to a steel with excellent sulfide stress corrosion cracking resistance (hereinafter referred to as 5 SCC resistance) obtained by direct quenching and tempering.

(従来の技術とその問題点) 近年、サワーガス、サワーオイルのガス田、油田が多く
開発されるようになり、これに伴って耐88CC%性の
優れた油井管用鋼材が求められている。
(Prior art and its problems) In recent years, many gas fields and oil fields for sour gas and sour oil have been developed, and along with this, there is a demand for steel materials for oil country tubular goods having excellent resistance to 88 CC%.

降伏強度50〜8012級のこの種鋼材として、従来で
は、C−8i−Fdn鋼もしくはC−8i−鳩−Or−
Mo鋼を焼入れ焼戻し処理することにより製造されてい
るが、これらの鋼材は、現在においても次のような問題
があった。
Conventionally, C-8i-Fdn steel or C-8i-Or-
Although Mo steel is manufactured by quenching and tempering, these steel materials still have the following problems.

■C−8i−胤鋼では、降伏強度60〜80KIF/−
級の高強度鋼において充分な耐SSCC特性が得られて
いない。
■C-8i-tane steel has a yield strength of 60 to 80KIF/-
Sufficient SSCC resistance properties have not been obtained in high-strength steels of this grade.

■C−S i −Mn −Cr −Mo鋼はC−8i 
−1’vln鋼より高い耐5scc特性が得られている
が、添加Cr、Mo量が多いため、製造コスト高となる
のを避けられない。
■C-S i -Mn -Cr -Mo steel is C-8i
Although a higher 5scc resistance than -1'vln steel is obtained, since the amounts of added Cr and Mo are large, it is inevitable that the manufacturing cost will be high.

■サワーガス、サワーオイルにおける腐食環境条件はま
すます厳しくなりつつあり、C−8i −Mn −Cr
 −Mo鋼においてもより高い耐SSCC特性が求めら
れているが、これに十分に答えることができない。
■Corrosive environmental conditions in sour gas and sour oil are becoming increasingly severe, and C-8i -Mn -Cr
-Mo steel is also required to have higher SSCC resistance, but this cannot be satisfactorily met.

(問題点を解決するための手段) 本発明は上記のような実情から研究を重ねて創案された
もので、その目的とするところは、低合金鋼の範囲にお
いて、直接焼入れプロセスによる組織制御を利用して従
来と同強度水準を確保しつつしかもより優れた耐5sc
c特性を持つ鋼を提供することにある。
(Means for Solving the Problems) The present invention was devised through repeated research in view of the above-mentioned circumstances, and its purpose is to achieve microstructural control by a direct quenching process in the range of low-alloy steels. Utilizes it to maintain the same strength level as before, yet with a superior 5sc resistance.
The objective is to provide steel with c characteristics.

この目的を達成するため、本発明は所定成分組成の鋼を
熱間加工後、直接焼入れ焼戻しした焼戻しマルテンサイ
ト組織の旧オーステナイト粒展伸度に右目しこれを規定
したもので、すなわち、C: 0.15〜0.35 w
t%、S皿=0.01〜0.50 wt %、Mn :
 0.4〜2.0 wt % 、 5otAL: 0.
001〜0.10wt%、残部Feおよび不可避的不純
物の基本組成を有するとともに、必要に応じ1 wt 
%以下のCu%1wt%以下のNi、2wt%以下のC
r、2wt%以下のMo、0.1wtチ以下(D Nb
 、 0.2wt %以下CD V 、 0.1wt 
%以下のTi、 0.1wtチ以下のREM、 0.1
 wt %以下のCaの一攬又は二種以上を添加した鋼
をAc。
In order to achieve this object, the present invention focuses on and defines the prior austenite grain elongation of a tempered martensitic structure obtained by directly quenching and tempering steel with a predetermined composition after hot working, that is, C: 0.15~0.35w
t%, S plate = 0.01-0.50 wt%, Mn:
0.4-2.0 wt%, 5otAL: 0.
001 to 0.10 wt%, the balance being Fe and unavoidable impurities, and if necessary 1 wt%
% or less Cu% 1wt% or less Ni, 2wt% or less C
r, 2wt% or less Mo, 0.1wt or less (D Nb
, 0.2wt % or less CD V , 0.1wt
% or less Ti, 0.1wt or less REM, 0.1
Ac refers to steel to which one or more types of Ca are added in an amount of wt % or less.

変態点以上で熱間加工後直接焼入れし、その後Act 
5i態点以下で焼戻しすることによって得られる焼戻し
マルテンサイト組織において、凡=(圧延方向の旧オー
ステナイト粒径dt、)/(肉厚方向の旧オーステナイ
ト粒径aZ)によって示される旧オーステナイト粒展伸
度を2以上とすることを特徴とするものである。
Directly quenched after hot working above the transformation point, then Act
In the tempered martensitic structure obtained by tempering below the 5i state, the prior austenite grain elongation is expressed by: = (prior austenite grain size dt in the rolling direction)/(prior austenite grain size aZ in the wall thickness direction) It is characterized by having a degree of 2 or more.

以下本発明を詳述する。The present invention will be explained in detail below.

まず本発明者らは、耐5scc特性を向上させる冶金的
因子の一つとして、結晶粒(焼入れ焼戻し処理を受けた
低合金鋼の場合旧オーステナイト粒)の形状に注目した
。そして、旧オーステナイト粒の形状の耐5scc特性
に及ぼす影響を見るため、熱間加工条件を変化させるこ
とにより旧オーステナイト粒形状を制御できる直接焼入
れ一焼戻し処理を施した鋼材の耐SSCC特性について
検討した。
First, the present inventors focused on the shape of crystal grains (prior austenite grains in the case of low alloy steel that has undergone quenching and tempering treatment) as one of the metallurgical factors that improves the 5 SCC resistance. Then, in order to examine the influence of the shape of prior austenite grains on the 5SCC resistance, we investigated the SSCC resistance of steel materials subjected to direct quenching and tempering treatment, in which the shape of prior austenite grains can be controlled by changing the hot working conditions. .

第11は0.2IC−0,228i−1,32Mn鋼(
YS=74〜76 K17wm” )について、圧延仕
上り後15秒後直接焼入几を行った場合の耐5scc特
性に及ぼす非再結晶温度領域の圧下率を示すものである
No. 11 is 0.2IC-0,228i-1,32Mn steel (
YS=74 to 76K17wm"), the rolling reduction ratio in the non-recrystallization temperature range on the 5 SCC resistance property when directly quenched 15 seconds after finishing rolling is shown.

この第1因から明らかなように、直接焼入れ焼戻し条件
において、未再結晶温度領域の圧下率を30チ以上とす
ると、旧オーステナイト粒径の展伸[R(圧延方向の旧
オーステナイト粒径dL/  肉厚方向の旧オーステナ
イト粒径dz )が2以上となり、この領域で 耐SS
CC特性(この場合、0.5%酢酸のH,S飽和溶液中
の三点曲げ試験における割れ発生限界応力Sc値)が向
上している。
As is clear from this first factor, under direct quenching and tempering conditions, if the rolling reduction in the non-recrystallized temperature region is 30 inches or more, the elongation of the prior austenite grain size [R (prior austenite grain size in the rolling direction dL/ The prior austenite grain size dz in the wall thickness direction is 2 or more, and in this region SS resistance
The CC characteristics (in this case, the critical cracking stress Sc value in a three-point bending test in a 0.5% acetic acid H, S saturated solution) are improved.

一方、未再結晶域圧下率を30−以下にすると、旧オー
ステナイト粒径の展伸度が2以下となり、SC値の向上
は余り大きくない。
On the other hand, when the reduction rate in the non-recrystallized region is set to 30 or less, the degree of elongation of the prior austenite grain size becomes 2 or less, and the improvement in the SC value is not so large.

本発明はこの知見に基づくもので、旧オーステナイト粒
の展伸化により耐5sccI¥f性の改善されるのは、
鋼材表面で発生した割れの肉厚方向への伝播が圧延方向
に展伸した旧オーステナイト粒界に沿ってそらされやす
いことに帰因しており、旧オーステナイト展伸度Rが2
以下では耐SSCC特性の向上に有効でない。
The present invention is based on this knowledge, and the reason why the 5scc I¥f resistance is improved by elongation of prior austenite grains is as follows.
This is due to the fact that the propagation of cracks generated on the steel surface in the thickness direction is easily deflected along the prior austenite grain boundaries extended in the rolling direction, and the prior austenite elongation rate R is 2.
If it is less than that, it is not effective in improving the SSCC resistance characteristics.

しかして、耐5scc特性向上に有効な旧オーステナイ
ト粒の展伸は、微量のNbやTiの添加によって促進さ
れる。第2図は0.2C−0,2Si −1,3Mn−
Nb鋼(YS=74〜76Si5において、Nb添加の
影響を検討した結果を示すもので、耐SSCC特性は、
同一の熱間圧延−直接焼入れ焼戻し条件においても、微
量Nb添加により顕著に改善されている。
Therefore, the elongation of prior austenite grains, which is effective in improving the 5 SCC resistance, is promoted by the addition of a small amount of Nb or Ti. Figure 2 shows 0.2C-0,2Si-1,3Mn-
This shows the results of examining the effect of Nb addition on Nb steel (YS=74-76Si5), and the SSCC resistance properties are as follows:
Even under the same hot rolling-direct quenching and tempering conditions, the addition of a small amount of Nb significantly improved the results.

すなわち、Nb無添加鋼では、圧延条件■(900℃以
下の圧下率70%、圧延仕上り温度870℃)のときだ
け展伸度R)2となり、圧延条件■(1000℃以下の
圧下率70%、圧延仕上り温度920℃)では几〈2と
なる。
In other words, for Nb-free steel, the elongation R) is 2 only under rolling conditions (1) (70% rolling reduction at 900°C or lower, finishing rolling temperature 870°C); , the rolling finish temperature is 920°C), the value becomes <2.

これに対し、Nb@加鋼では、両圧延条f’FともR>
2となり、そのような条件において耐5scc特性はい
ずれも顕著に改善されることがわかる。
On the other hand, in Nb@processed steel, both rolled strips f'F have R>
2, and it can be seen that the 5scc resistance characteristics are all significantly improved under such conditions.

このような旧オーストナイト粒の展伸化による耐5sc
c特性の改善効果は、後述する実施例に示すように、C
−Si −Mn −Cr−kio鋼(例えば、0.3 
C−0,2S i −0,5Mn−I Cr −0,5
Mo鋼)においても得られることはもとよりである。
5sc resistance due to elongation of such prior austonite grains
The effect of improving the c characteristic is as shown in the examples described later.
-Si -Mn -Cr-kio steel (e.g. 0.3
C-0,2S i -0,5Mn-I Cr -0,5
Of course, it can also be obtained with Mo steel).

以上のような点から、本発明は先に述べたような構成を
採用したもので、その限定理由を以下に述べる。
In view of the above points, the present invention adopts the configuration described above, and the reasons for the limitations will be described below.

Cは直接焼入れによって完全硬化組織を得るには、0.
15Wt 4以上必要であり、また、直接焼入れによっ
て焼割れを防止するには0.35wt%以下である必要
があるためである。
C must be 0.0 to obtain a completely hardened structure by direct quenching.
This is because 15 Wt 4 or more is required, and in order to prevent quench cracking by direct quenching, it needs to be 0.35 wt % or less.

8iは溶鋼の脱酸を完全にするためには、0.01wt
 4以上必要であるが、0.5wt 4以上の含有は鋼
材の延靭性を害するためである。
8i is 0.01wt to completely deoxidize molten steel.
4 or more is necessary, but the content of 0.5wt4 or more is because it impairs the ductility and toughness of the steel material.

Mnは鋼材の焼入性確保の観点より0.4wt係以上が
必要であるが、2wt%以上の含有は鋼材の延靭性およ
び耐5scc特性を損うため規定した。
Mn needs to be at least 0.4 wt % from the viewpoint of ensuring the hardenability of the steel material, but it is specified because the content of 2 wt % or more impairs the ductility and 5 SCC resistance of the steel material.

5otAtは溶鋼の脱酸を完全にするためには0.00
1wt%以上必要であるが、0.1wt tip以上の
含有は鋼材の延靭性を損うためである。
5otAt is 0.00 in order to completely deoxidize molten steel.
Although 1 wt% or more is required, the content of 0.1 wt tip or more impairs the ductility and toughness of the steel material.

Nb、 Tiは既述のように旧オーステナイト粒の展伸
化を促進するのに有効な元素であるが、0.1wt%を
越える添加は効果が飽和となるため上限を規定した。
As mentioned above, Nb and Ti are effective elements for promoting elongation of prior austenite grains, but if added in excess of 0.1 wt%, the effect becomes saturated, so an upper limit was specified.

Cu、 Ni、 Cr、 Moはそれぞれ限定値以下の
添加により耐88CC特性を損わずに焼入性を向上する
と共に、固溶強化、析出強化により材料強度を高めるこ
とができるが、限定値を越える添加は製造コストの観点
から望ましくない。
Cu, Ni, Cr, and Mo can be added in amounts below their respective limits to improve hardenability without impairing the 88CC resistance, and to increase material strength through solid solution strengthening and precipitation strengthening. Addition in excess of this amount is undesirable from the viewpoint of manufacturing costs.

■は0.2wtチ以下の添加により、耐5scc特性を
損うことなく析出強化を通して材料強度を高めるが、0
.2wt%以上の添加は製造コストの観点から望ましく
ない。
By adding 0.2wt or less, ■ increases material strength through precipitation strengthening without impairing 5scc resistance properties,
.. Addition of 2 wt% or more is undesirable from the viewpoint of manufacturing cost.

REM、 Caは限定値以下の添加によりMn8介在物
の形態を球状化し、鋼材の延靭性を改善するが、限定値
以上の添加はかえって延靭性を害し、また、耐5scc
特性に対しては影響を与えないからである。
REM, Ca makes the morphology of Mn8 inclusions spherical and improves the ductility of the steel material when added below the limited value, but when added above the limited value, it actually impairs the ductile toughness and also reduces the 5scc resistance.
This is because it does not affect the characteristics.

本発明は上記の限定された組成の鋼を直接焼入れプ1フ
セスにより組織制御し、焼戻しマルテンサイト組織にお
いて、旧オーステナイト粒展伸g R= dL/dz 
) 2とする。この理由は既述のとおりであるが、付言
するならば、未再結晶領域の熱間力Ω工によって得られ
る展伸した旧オーステナイト粒は、直接焼入れ処理によ
って始めて保存されるものであり、再加熱焼入れ処理に
よっては展伸した旧オーステナイト粒は得られない。
The present invention controls the structure of steel with the above-mentioned limited composition by direct quenching process, and in the tempered martensitic structure, prior austenite grain elongation g R = dL/dz
) 2. The reason for this has already been mentioned, but it should be added that the elongated prior austenite grains obtained by hot mechanical processing in the non-recrystallized region are preserved only by direct quenching, and cannot be recycled. Expanded prior austenite grains cannot be obtained by heating and quenching.

(実施例) 次に本発明の具体的な実施例を比較例と共に示す。(Example) Next, specific examples of the present invention will be shown together with comparative examples.

まず、本発明鋼と比較鋼の化学取分を第1第    1
    表 第2表は第1表に示す各鋼の熱間圧延、熱処理条件と旧
オーステナイト粒の展伸度、降伏強さ及び耐5scc特
性の検討結果を示すものである。
First, the chemical fractions of the inventive steel and comparative steel are calculated as follows:
Table 2 shows the hot rolling and heat treatment conditions of each steel shown in Table 1, as well as the results of examination of the degree of elongation of prior austenite grains, yield strength, and 5 SCC resistance properties.

上記第1表及び第2表から、不発明鋼においては、Nb
添加の有無にかかわらず、旧オーステナイト粒展伸度が
2以上となっているが、比較鋼はいずれも旧オーステナ
イト粒展伸度が2以下となっている。そして、本発明鋼
はいずれもそれぞれ対応する比較鋼に比べ、略強度的に
同等であって、しかも優れた耐5scc特性が得られて
いる。
From Tables 1 and 2 above, in non-inventive steel, Nb
Regardless of the presence or absence of addition, the prior austenite grain expansion elongation is 2 or more, but the prior austenite grain expansion elongation of all comparative steels is 2 or less. All of the steels of the present invention have approximately the same strength as the corresponding comparative steels, and have excellent 5scc resistance characteristics.

(発明の効果) 以上説明した本発明によるときには、必要な強度水準を
保ちつつ、しかも優れた耐5scc特性を備えた鋼とす
ることができ、ことに低合金鋼の範囲において優れた耐
5SCC特性の鋼材とすることができるため、サワーガ
ス、サワーオイルのガス田、油田等における油井管用鋼
材として好適なものを提供できるものである。
(Effects of the Invention) According to the present invention as described above, it is possible to obtain a steel that maintains the required strength level and has excellent 5SCC resistance, especially in the range of low alloy steel. Therefore, it is possible to provide a steel material suitable as a steel material for oil country tubular goods in gas fields, oil fields, etc. for sour gas and sour oil.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は耐5scc特性に及ぼす未再結晶温度領域の圧
下率の影響を示すグラフ、第2図は耐5scc特性に及
ばすNb添加の影響を示すグラフである。
FIG. 1 is a graph showing the influence of the rolling reduction in the non-recrystallization temperature range on the 5 SCC resistance characteristics, and FIG. 2 is a graph showing the influence of Nb addition on the 5 SCC resistance characteristics.

Claims (1)

【特許請求の範囲】 C:0.15〜0.35wt%、Si:0.01〜0.
50wt%、Mn:0.4〜2.0wt%、SolAl
:0.001〜0.10wt%、残部Feおよび不可避
的不純物の基本組成を有するとともに、必要に応じ 1wt%以下のCu、1wt%以下のNi、2wt%以
下のCr、2wt%以下のMo、0.1wt%以下のN
b、0.2wt%以下のV、0.1wt%以下のTi、
0.1wt%以下のREM、0.1wt%以下のCaの
一種又は二種以上を添加した鋼を、Ac_3変態点以上
で熱間加工後直接焼入れし、その後Ac_1変態点以下
で焼戻しすることによつて得られる焼戻しマルテンサイ
ト組成 において、R=(圧延方向の旧オーステナ イト粒径d_L)/(肉厚方向の旧オーステナイト粒径
d_Z)によつて示される旧オーステナイト粒展伸度を
2以上とすることを特徴と する直接焼入れ焼戻しによる耐SSCC特性の優れた鋼
[Claims] C: 0.15-0.35 wt%, Si: 0.01-0.
50wt%, Mn: 0.4-2.0wt%, SolAl
: 0.001 to 0.10 wt%, balance Fe and unavoidable impurities basic composition, and if necessary, 1 wt% or less Cu, 1 wt% or less Ni, 2 wt% or less Cr, 2 wt% or less Mo, N less than 0.1wt%
b, V of 0.2 wt% or less, Ti of 0.1 wt% or less,
Steel to which 0.1 wt% or less of REM and 0.1 wt% or less of Ca are added is directly quenched after hot working at a temperature above the Ac_3 transformation point, and then tempered at a temperature below the Ac_1 transformation point. In the tempered martensite composition thus obtained, the prior austenite grain expansion elongation represented by R = (prior austenite grain size d_L in the rolling direction)/(prior austenite grain size d_Z in the wall thickness direction) is 2 or more. A steel with excellent SSCC resistance due to direct quenching and tempering.
JP16861985A 1985-08-01 1985-08-01 Directly quenched and tempered steel having superior sscc resistance characteristic Granted JPS6230849A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16861985A JPS6230849A (en) 1985-08-01 1985-08-01 Directly quenched and tempered steel having superior sscc resistance characteristic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16861985A JPS6230849A (en) 1985-08-01 1985-08-01 Directly quenched and tempered steel having superior sscc resistance characteristic

Publications (2)

Publication Number Publication Date
JPS6230849A true JPS6230849A (en) 1987-02-09
JPH049847B2 JPH049847B2 (en) 1992-02-21

Family

ID=15871416

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16861985A Granted JPS6230849A (en) 1985-08-01 1985-08-01 Directly quenched and tempered steel having superior sscc resistance characteristic

Country Status (1)

Country Link
JP (1) JPS6230849A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6453718A (en) * 1987-07-27 1989-03-01 Tool For Bendengu Inc Method and device for bending pipe
JPH04362157A (en) * 1991-06-07 1992-12-15 Japan Steel Works Ltd:The Steel for welding structure excellent in sulfide stress corrosion cracking resistance and low temperature toughness
US5938865A (en) * 1995-05-15 1999-08-17 Sumitomo Metal Industries, Ltc. Process for producing high-strength seamless steel pipe having excellent sulfide stress cracking resistance

Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5471714A (en) * 1977-11-21 1979-06-08 Nippon Kokan Kk <Nkk> Manufacture of control-rolled high tensile steel with no separation
JPS54119324A (en) * 1978-03-08 1979-09-17 Kawasaki Steel Co Production of steel pipe for oil well
JPS54124817A (en) * 1978-03-23 1979-09-28 Nippon Kokan Kk <Nkk> Steel of excellent sulfide resistance and excellent corrosion crack resistance
JPS5613463A (en) * 1979-07-10 1981-02-09 Sumitomo Metal Ind Ltd Line pipe steel with superior hydrogen sulfide crack resistance
JPS5613462A (en) * 1979-07-10 1981-02-09 Sumitomo Metal Ind Ltd Line pipe steel with superior hydrogen sulfide crack resistance
JPS56119759A (en) * 1980-02-28 1981-09-19 Nippon Kokan Kk <Nkk> High tensile steel with superior sulfide corrosion crack resistance
JPS589919A (en) * 1981-07-09 1983-01-20 Kawasaki Steel Corp Production of high tensile hot rolled steel strip of superior low temperature toughness
JPS5858252A (en) * 1981-10-02 1983-04-06 Kawasaki Steel Corp Steel for steel pipe for oil well
JPS58107476A (en) * 1981-12-19 1983-06-27 Kawasaki Steel Corp High tensile steel excellent sulfide stress corrosion cracking resistance
JPS58199818A (en) * 1982-05-17 1983-11-21 Nippon Steel Corp Manufacture of high strength steel pipe for oil well
JPS58204159A (en) * 1982-05-24 1983-11-28 Japan Steel Works Ltd:The Sulfide crack resistant thick steel with superior weldability
JPS5913052A (en) * 1982-02-19 1984-01-23 Kawasaki Steel Corp Stainless steel material with high strength and superior resistance to corrosion, stress corrosion cracking and cracking due to sulfide and its manufacture
JPS6067620A (en) * 1983-09-21 1985-04-18 Kobe Steel Ltd Preparation of steel plate
JPS6096718A (en) * 1983-10-31 1985-05-30 Kobe Steel Ltd Manufacture of steel sheet excellent in resistances to hydrogen inducing cracking and stress corrosion crcking

Patent Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5471714A (en) * 1977-11-21 1979-06-08 Nippon Kokan Kk <Nkk> Manufacture of control-rolled high tensile steel with no separation
JPS54119324A (en) * 1978-03-08 1979-09-17 Kawasaki Steel Co Production of steel pipe for oil well
JPS54124817A (en) * 1978-03-23 1979-09-28 Nippon Kokan Kk <Nkk> Steel of excellent sulfide resistance and excellent corrosion crack resistance
JPS5613463A (en) * 1979-07-10 1981-02-09 Sumitomo Metal Ind Ltd Line pipe steel with superior hydrogen sulfide crack resistance
JPS5613462A (en) * 1979-07-10 1981-02-09 Sumitomo Metal Ind Ltd Line pipe steel with superior hydrogen sulfide crack resistance
JPS56119759A (en) * 1980-02-28 1981-09-19 Nippon Kokan Kk <Nkk> High tensile steel with superior sulfide corrosion crack resistance
JPS589919A (en) * 1981-07-09 1983-01-20 Kawasaki Steel Corp Production of high tensile hot rolled steel strip of superior low temperature toughness
JPS5858252A (en) * 1981-10-02 1983-04-06 Kawasaki Steel Corp Steel for steel pipe for oil well
JPS58107476A (en) * 1981-12-19 1983-06-27 Kawasaki Steel Corp High tensile steel excellent sulfide stress corrosion cracking resistance
JPS5913052A (en) * 1982-02-19 1984-01-23 Kawasaki Steel Corp Stainless steel material with high strength and superior resistance to corrosion, stress corrosion cracking and cracking due to sulfide and its manufacture
JPS58199818A (en) * 1982-05-17 1983-11-21 Nippon Steel Corp Manufacture of high strength steel pipe for oil well
JPS58204159A (en) * 1982-05-24 1983-11-28 Japan Steel Works Ltd:The Sulfide crack resistant thick steel with superior weldability
JPS6067620A (en) * 1983-09-21 1985-04-18 Kobe Steel Ltd Preparation of steel plate
JPS6096718A (en) * 1983-10-31 1985-05-30 Kobe Steel Ltd Manufacture of steel sheet excellent in resistances to hydrogen inducing cracking and stress corrosion crcking

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6453718A (en) * 1987-07-27 1989-03-01 Tool For Bendengu Inc Method and device for bending pipe
JPH04362157A (en) * 1991-06-07 1992-12-15 Japan Steel Works Ltd:The Steel for welding structure excellent in sulfide stress corrosion cracking resistance and low temperature toughness
US5938865A (en) * 1995-05-15 1999-08-17 Sumitomo Metal Industries, Ltc. Process for producing high-strength seamless steel pipe having excellent sulfide stress cracking resistance

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